Log In|Sign Up
中文
在11号染色体上，通过CRISPR/Cas9系统和sgRNA5'-GGGATCTTCGTCTTCTGACG-3'设计，产生了一个26个碱基对的缺失，位置在60,778,048-60,778,073，具体在Smcr8基因的第1外显子。这个缺失导致了一个预测的移位蛋白质产物，从氨基酸7开始产生，直到包含6个异常氨基酸后终止。(来源：J:268243)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
